Multimodal Analgesia Effect on Post Surgical Patient
a study on Obesity Surgery Bariatric Surgery
Summary
- Eligibility
- for females ages 35-65 (full criteria)
- Location
- at UC Davis
- Dates
- study startedcompletion around
Description
Summary
Patients undergoing Bariatric Surgery at the University of California Davis Medical Center will be divided into two groups, one receiving Standard of Care pain control medications vs the second group which will receive non-narcotic pain medications with rescue pain medications available if needed
Details
Pain control after weight loss surgery is challenging due to the alteration of digestive system anatomy and limitation on using medications which can either be crushed or in liquid form for the first 10 days to 14 days after surgery. Additionally there are multiple programs in place to eliminate the use of narcotic/opioid based pain medications due their potential addictive risks.
This study compares two groups of patients whom will have Roux en Y Gastric Bypass Surgery at UC Davis Medical Center, the control group will receive standard of care pain control medications (including opioid based medications) compared to the research arm, this group will receive Gabapentinin and Tylenol for pain control after surgery with rescue pain medications available if needed.
Post surgery both groups will be managed by the Bariatric Surgery Team and will be contacted periodically as part of the standard of care to monitor pain control and usage of any rescue medications (if needed).
Keywords
Obesity, Morbid, Surgery, Bariatric Surgery Candidate, Bariatric Surgery,, Pain Control, Gabapentinin, Morbid Obesity, Acetaminophen, Scopolamine, Oxycodone, Gabapentin, Hydromorphone, Hydrocodone, Bupivacaine, Cyclobenzaprine, Butylscopolammonium Bromide, Neurontin, Dilaudid Injectable Product, Marcaine Injectable Product, Oxycodone Hydrochloride, Hycet 7.5Mg-325Mg/15Ml Solution, Zofran Injection, Scopolamine patch, Ativan, Flexeril Oral Product, Tylenol Suspension, Multi-Modal
Eligibility
You can join if…
Open to females ages 35-65
- Women who undergo index weight loss procedures at UC Davis Medical Center
- Women with a BMI =>30
- Age from 35-65
- American Society of Anesthesiology (ASA) score of 3 or less
- No previous history of prior abdominal/foregut surgery
You CAN'T join if...
- Not having an index weight los surgery for obesity
- Do not meet the NIH Standards for weight loss surgery
- Additional planned or unplanned procedures during the index surgical procedure such as Cholecystectomy or extensive lysis of adhesions (>30 minutes)
- BMI < 30
- Men
- Women considering or currently planning on gender altering/modification
- ASA score of 4 or higher
- Patients less than 35 years of age or older than 65 years of age at the time of surgical consent
- A history of open abdominal surgery including umbilical, ventral, or splengalic hernia repair with or without mesh implantation, transplant or vascular surgery or any foregut procedures including hiatal hernia repair or anti-reflux surgery
- Arthritis, Fibromyalgia, chronic pain syndrome
- Other conditions requiring daily use of oral pain medications
- Prisoners
- Allergy to Gabapentin
Location
- UC Davis Health
accepting new patients
Sacramento California 95817 United States
Details
- Status
- accepting new patients
- Start Date
- Completion Date
- (estimated)
- Sponsor
- University of California, Davis
- ID
- NCT04240626
- Phase
- Phase 4 research study
- Study Type
- Interventional
- Participants
- Expecting 60 study participants
- Last Updated